A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622107



Internal ID6662277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1572350..1573239hg38UCSC Ensembl
Innerchr10:1572385..1573205hg38UCSC Ensembl
Outerchr10:1572316..1573274hg38UCSC Ensembl
chr10:1614545..1615434hg19UCSC Ensembl
Innerchr10:1614580..1615400hg19UCSC Ensembl
Outerchr10:1614511..1615469hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13665703, essv13665704
SamplesHG01851, HG03814
Known GenesADARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622107
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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